US3499721A - Stabilized composition of p-quinonedihaloimine compound - Google Patents
Stabilized composition of p-quinonedihaloimine compound Download PDFInfo
- Publication number
- US3499721A US3499721A US572913A US3499721DA US3499721A US 3499721 A US3499721 A US 3499721A US 572913 A US572913 A US 572913A US 3499721D A US3499721D A US 3499721DA US 3499721 A US3499721 A US 3499721A
- Authority
- US
- United States
- Prior art keywords
- compound
- composition
- quinonedihaloimine
- agent
- paste
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/008—Preparing dyes in situ
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/32—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using oxidation dyes
Definitions
- the present invention relates to a stabilized composition of p-quinonedihaloimine compound.
- p-quinonedihaloimine compound is useful for dyeing hydrophobic fibers or moulded product of synthetic resin, such as polyolefin.
- this compound is unstable and has a tendency to decompose during production, storage and dyeing, particularly, in the presence of water.
- the compound decomposes vigorously at a higher temperature than 120 C. in the refined state, and it has a toxicity to skin, for example it causes eruptions.
- the present inventors have discovered that the stability of p-quinonedihaloimine compound is remarkably improved by adding a bulfer agent such asalkali metal phosphates and alkali metal acetate to maintain the pH- wherein X represents a halogen atom chosen from chlorine and bromine and nucleus A may be substituted with methyl, methoxy or a halogen atom chosen from chlorine and bromine, and at least one buffer agent chosen from alkali metal phosphates and alkali metal acetates, which maintain the pH-value of an aqueous solution at 5 to 8, and if required, the said composition containing a dispersing agent, and an inert agent, and the said composition being in the form of paste, granules, dry powder and suspension.
- a bulfer agent such asalkali metal phosphates and alkali metal acetate
- the p-quinonedihaloimine compound is easily obtained by known method, for example, by oxidizing the corresponding para-phenylenediamine compound with sodium hypochlorite, or calcium hypochlorite.
- the p-quinonedihaloiminecompound employed in the present invention includes, for example, 1,4-benzoquinonedichlorimide, 1,4 benzoquinonedibromimine, and 2-methyl-, 2-methoxy-, .2-chloro-, 2-bromo-, 2,5-dimethyl-, 2,5-dichloro-, 2,6-dichloro-, 2,6-dibromo, 2,3,6-trichloro-, 2,3,5,6-tetrachloro-derivatives thereof.
- the buffer agent employed in the present invention includes, for example, disodium hydrogenphosphate, dipotassium hydrogenphosphate, sodium dihydrogen phosphate, potassium dihydrogenphosphate and sodium acetate and mixtures thereof which maintains the pH value of an aqueous suspension of the composition at 5-8.
- the buffer agent may be employed as either anhydrous crystal or hydrous crystal and also as an aqueous solution in case the composition is an aqueous dispersion.
- the storage stability of p-quinonedihaloimine compound is improved somewhat by the addition of a trace amount of the buffer agent, however, it is preferable that the buffer agent is added to the p-quinonedihaloimine compound in an amount of from 1% to by Weight based on the weight of the p-quinonedihaloimine compound, and practically a suitable storage stability may be obtained by the addition of the buffer agent in an amount of from 5% to 10% by weight based on the weight of p-quinonedihaloimine compound.
- the amount of the buffer agent added is varied depending upon the kind or concentration of the p-quinonedihaloimine compound in the composition, and further depending upon the other components present such as dispersing agent.
- the buffer agent contained in the composition also Works as a dyeing assistant in the dyeing bath, and it is not'necessary to add a dyeing assistant of this kind during dyeing, if enough of the buffer agent has been added previously to the composition, and as a result of this fact compositions of this invention are convenient for later practical use. From these views of the stabilizing action thereof and of the practical use,
- a large amount of a buffer agent is added inthe composition.
- the added amount of the anhydrous, metal phosphate must be varied depending on the amount of the water contained in the paste of the p-quinonedihaloimine.
- the composition of the present invention may be obtained by merely mixing the said p-quinonedihaloimine compound and the buffer agent.
- the buffer agent may be added to the quinonedihalimide compound at any convenient time, that is, before the reaction for the synthesis of p-quinonedihaloimine compound, during the reaction, before the isolation of the product after the reaction is over, at the isolation of the product, for example, by washing the product in a filter with a buffer agent aqueous solution, or during mixing of the product with a dispersing agent or during peptizing.
- the buffer agent may be added during or after milling the p-quinonedihaloimine compound.
- the pH of the suspension or the paste of the p-quinonedihaloimine compound is nearly neutral prior to mixing with the buffer agent, and it is preferable, if necessary, that the p-quinonedihaloimine compound is purified or neutralized before adding the buffer agent.
- a composition is produced in the form that the p-quinonedihaloimine compound is well dispersed in water, and therefore it is necessary that the composition is well mixed or peptized with a suitable dispersing agent in a wet or dry process according to a known manner.
- the various kinds of dispersing agents such as anionic or nonionic surfactant may be employed without affecting the stability of the composition.
- the dispersing agents include formalin condensation product of alkylnaphthalenesulfonic acid, salts of alkylbenzenesulfonic acid or alkylnaphthalenesulfonic acid, a sulfuric acid es ters of polycondensation product of ethylene oxide and alcohols or alkylphenols, sulfuric acid esters of higher alcohols, ligninsulfonate, and alkylphenyl ethers of polyethyleneglycol.
- the formalin condensation product of alkyl naphthalenesulfonic acid is especially preferable.
- the present composition may further contain an inorganic or organic water-soluble adding agent, which preferably, gives a neutral aqueous solution of the present composition, for example, sodium sulfate, sodium chloride, cane sugar, dextrin and carboxymethyl cellulose.
- an inorganic or organic water-soluble adding agent which preferably, gives a neutral aqueous solution of the present composition, for example, sodium sulfate, sodium chloride, cane sugar, dextrin and carboxymethyl cellulose.
- the paste is prepared by mixing the wet p-quinonedihaloimine compound, the buffer agent, and if necessary, the dispersing agent and adding agent, in an optional order.
- the paste prepared by mixing in the presence of water has a high caking property and can not be made into granules of the composition by the mere addition of various water-soluble adding agent in order to increase the viscosity thereof.
- a paste having a low caking property may be obtained, however, the composition is not readily dispersible in water and therefore is not desirable for practical use.
- the above difficulty in the process of formation of granules of the composition due to the caking property is overcome by the procedure wherein all or part of the buffer agent is added in an anhydrous form, such as anhydrous sodium or potassium dihydrogenphosphate, anhydrous disodium or dipotassium hydrogenphosphate, which is useful as a stabilizer.
- anhydrous metal phosphate is added into the aqueous paste Containing a p-quinonedihaloimine compound, a dispersing agent and an adding agent and well mixed, the caking property of the paste gradually disappears and the composition becomes suitable for making granules.
- the reason for the above phenomena is considered to be that all or a part of the employed anhydrous metal phosphate gets water from the paste as crystal water thereby changing to hydrous metal phosphate, raising the viscosity of the composition, and decreasing the caking property thereof.
- the suspension of the present composition may be prepared by mixing water, a p-quinonedihaloimine compound and a buffer agent and, if necessary, further a dispersant and an adding agent, or by adding and mixing water to the paste of the present composition.
- composition of the present invention may be measured by a quantitative analysis of the p-quinonedihaloirnine compound in the course of the elapse of time.
- the p-quinonedihaloimine compound contained in the present composition is more stable than the free pquinonedihaloimine compound itself.
- the paste of the present composition is substantially stable for three months at room temperature, while the wet pquinonedihaloimine compound cake which contains no buffer agent is almost decomposed during the storage of three months, even when pH of Water suspension prepared from it is in the range of 5-8 at the start of its storage.
- EXAMPLE 1.-PASTE 1 As pure compound. The above ingredients were mixed to form paste according to the known procedure.
- the method for making granules of the composition according to the present invention is as follows. A wet paste of a p-quinonedihaloimine compound, a dispersing agent, and an alkali metal phosphate the whole or a part of which is anhydrous are placed in a kneader in optional order and well mixed, and thereafter the mixture is made into granules by various kinds of extruder type granulator and then dried. Further, if necessary, the granules are sifted.
- the granules of the composition are dried very easily because the granules are porous and have a very large surface area.
- the powder of the present composition may be prepared by mixing dried and powdered p-quinonedihaloimine compound with the buffer agent and if necessary further with a dispersant and other adding agent, or by drying the ing no buffer agent. These etfects are not disturbed by the addition of dispersing agent, such as the formalin condensation product of alkylnaphthalenesulfonic acid, and of an inert agent, such as carboxymethylcellulose.
- dispersing agent such as the formalin condensation product of alkylnaphthalenesulfonic acid
- an inert agent such as carboxymethylcellulose.
- Control means that the formation does not contain a bufier agent. As shown in Table 4, the stability of the water suspension of the present invention is superior to the water. suspension containing no buffer agent.
- Control means that the formulation does not contain a bufier agent.
- the above ingredients were well mixed to form a paste.
- the paste was dried and pulverized to form a dry powder.
- the stability of the water suspension of the present invention is superior to stability of the water suspension containing no butler agent.
- composition consisting essentially of a pquinonedihaloimine compound of the formula
- X represents a halogen atom chosen from chlorine and bromine and nucleus A may be substituted with methyl, methoxy or a halogen chosen from chlorine and bromine and an effective amount of at least one buffer agent chosen from alkali metal phosphates and alkali metal acetates, which maintains the pH-value of an aqueous solution at 5 to 8.
- composition according to claim 1 wherein the composition further contains'a dispersing agent.
- composition according to claim 1 wherein the composition further contains an inert agent.
- composition according to claim 1 wherein the p-quinonedihalomine compound is chosen from 1,4- benzoquinonedichlorimine and 1,4 benzoquinonedi- 8 bromimine and 2-methyl-, 2-methoxy-, 2-chloro-, 2- bromo-, .2,5-dimethyl-, 2,5-dichloro-, 2,6-dichloro-, 2,6- dibromo-, 2,3,6-trichloro- 2,3,5,6-tetrachloro-derivatives thereof.
- composition according to claim 1 wherein the buffer agent is chosen from disodium hydrogenphosphate, dipotassium hydrogenphosphate, sodium dihydrogenphosphate, potassium dihydrogenphosphate and sodium acetate and mixtures thereof.
- composition according to claim 1 wherein the composition is in the form of paste, granules, dry powder or water suspension.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5081765 | 1965-08-19 | ||
JP5081865 | 1965-08-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3499721A true US3499721A (en) | 1970-03-10 |
Family
ID=26391288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US572913A Expired - Lifetime US3499721A (en) | 1965-08-19 | 1966-08-17 | Stabilized composition of p-quinonedihaloimine compound |
Country Status (7)
Country | Link |
---|---|
US (1) | US3499721A (it) |
BE (1) | BE685707A (it) |
CH (1) | CH469675A (it) |
DE (1) | DE1593415A1 (it) |
ES (1) | ES330344A1 (it) |
GB (1) | GB1146749A (it) |
NL (2) | NL6611610A (it) |
-
0
- NL NL126581D patent/NL126581C/xx active
-
1966
- 1966-08-17 US US572913A patent/US3499721A/en not_active Expired - Lifetime
- 1966-08-17 GB GB36913/66A patent/GB1146749A/en not_active Expired
- 1966-08-18 BE BE685707D patent/BE685707A/xx unknown
- 1966-08-18 ES ES0330344A patent/ES330344A1/es not_active Expired
- 1966-08-18 CH CH1194466A patent/CH469675A/fr unknown
- 1966-08-18 DE DE19661593415 patent/DE1593415A1/de active Pending
- 1966-08-18 NL NL6611610A patent/NL6611610A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
BE685707A (it) | 1967-02-01 |
GB1146749A (en) | 1969-03-26 |
CH469675A (fr) | 1969-03-15 |
DE1593415A1 (de) | 1970-07-23 |
ES330344A1 (es) | 1967-06-16 |
NL6611610A (it) | 1967-02-20 |
NL126581C (it) |
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